JPH06505305A - metal recovery equipment - Google Patents
metal recovery equipmentInfo
- Publication number
- JPH06505305A JPH06505305A JP4504783A JP50478392A JPH06505305A JP H06505305 A JPH06505305 A JP H06505305A JP 4504783 A JP4504783 A JP 4504783A JP 50478392 A JP50478392 A JP 50478392A JP H06505305 A JPH06505305 A JP H06505305A
- Authority
- JP
- Japan
- Prior art keywords
- housing
- metal
- metal extraction
- electrode
- fluid inlet
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 229910052751 metal Inorganic materials 0.000 title claims description 62
- 239000002184 metal Substances 0.000 title claims description 62
- 238000011084 recovery Methods 0.000 title description 3
- 239000012530 fluid Substances 0.000 claims description 49
- 238000000605 extraction Methods 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 21
- 238000000926 separation method Methods 0.000 claims description 19
- 238000005363 electrowinning Methods 0.000 claims description 15
- 150000002739 metals Chemical class 0.000 claims description 12
- 239000004020 conductor Substances 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 7
- 238000003306 harvesting Methods 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims 1
- 239000010931 gold Substances 0.000 claims 1
- 229910052737 gold Inorganic materials 0.000 claims 1
- 239000007788 liquid Substances 0.000 description 25
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 16
- 229910052802 copper Inorganic materials 0.000 description 16
- 239000010949 copper Substances 0.000 description 16
- 239000007789 gas Substances 0.000 description 16
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 10
- 229910000831 Steel Inorganic materials 0.000 description 8
- 239000010959 steel Substances 0.000 description 8
- 239000002253 acid Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000002923 metal particle Substances 0.000 description 4
- 238000007789 sealing Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- OMZSGWSJDCOLKM-UHFFFAOYSA-N copper(II) sulfide Chemical compound [S-2].[Cu+2] OMZSGWSJDCOLKM-UHFFFAOYSA-N 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical compound [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 1
- 229910001245 Sb alloy Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000002140 antimony alloy Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/04—Extraction of metal compounds from ores or concentrates by wet processes by leaching
- C22B3/045—Leaching using electrochemical processes
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C7/00—Constructional parts, or assemblies thereof, of cells; Servicing or operating of cells
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C7/00—Constructional parts, or assemblies thereof, of cells; Servicing or operating of cells
- C25C7/002—Constructional parts, or assemblies thereof, of cells; Servicing or operating of cells of cells comprising at least an electrode made of particles
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Geology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Electrolytic Production Of Metals (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Water Treatment By Sorption (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)
- Extraction Or Liquid Replacement (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるため要約のデータは記録されません。 (57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】 本発明は、金属回収装置に関する。[Detailed description of the invention] The present invention relates to a metal recovery device.
本発明は、水性溶液から銅を電解採集する用途を有しており、図示目的のために その用途に説明されるが限定はしない。しかし、本発明は銀、あるいは他の金属 、あるいはガス物質のような他の用途に使用され得ることを理解されたい。The present invention has application in the electrowinning of copper from aqueous solutions and is for illustrative purposes only. Its use is described but not limited. However, the present invention does not require silver or other metals. It should be understood that it may be used for other applications such as, or gaseous materials.
鉱石から金属を抽出する多くの方法は、鉱石中に小さいけれども有意義な割合の 金属を残す。他の方法は、低いグレードの鉱石に経済的に利用できない。処理さ れた鉱石から残っている金属を抽出するひとつの確立された方法、あるいは低い グレードの鉱石から金属を抽出するひとつの確立された方法は、リーチングrl eachingJとして知られている。リーチングは抽出される金属が分解する 流体を鉱石中に通し、その流体を集め、そしてその金属をその流体から分離する 工程を含んでいる。鋼の抽出の場合において、典型的に使用される流体は硫化鋼 を製造するために銅と反応する稀硫酸である。Many methods of extracting metals from ores extract a small but meaningful percentage of the ore. Leave the metal behind. Other methods are not economically applicable to lower grades of ore. processed One established method for extracting remaining metals from mined ores is One established method of extracting metals from grade ores is leaching RL. It is known as eachingJ. Leaching causes the extracted metal to decompose passing a fluid through the ore, collecting the fluid, and separating the metal from the fluid Contains processes. In the case of steel extraction, the fluid typically used is sulfided steel. is dilute sulfuric acid that reacts with copper to produce .
硫化鉄と自由鋼が形成される場合、銅は金属鉄、あるいは鋼にそれを晒すことに よって鉱物から流れる硫化鋼から除去される。If iron sulfide and free steel are formed, copper will be exposed to metallic iron, or even steel. It is therefore removed from the sulfide steel flowing from the mineral.
運悪くそのようにして製造された銅は有意義な不純物を含んでおり、酸はそのプ ロセス中に使い果たされてしまい、そのプロセスの経済性を低下させる。その代 わりに硫化銅溶液が電解セル中に通されても良く、これによって自由鋼および硫 酸の両方を回収する。しかし、従来の電解セルは採集動作から得られる低い濃度 の流体から金属を直接採集する用途に経済的に適用できず、その流体が電解され る前に濃度を高めることが必要になる。Unfortunately, the copper produced in this way contains significant impurities, and the acid used up during the process, reducing the economics of the process. That cost Alternatively, a copper sulfide solution may be passed through the electrolytic cell, thereby removing the free steel and sulfur. Collect both acids. However, conventional electrolytic cells have low concentrations obtained from the collection operation. If the fluid is electrolyzed, it cannot be economically applied to the direct extraction of metals from It will be necessary to increase the concentration before
本発明は上に述べた問題点を無くし、信頼性があって有効な金属抽出装置を提供 することに目的がある。本発明の他の目的および利点は、以下、明らかになる。The present invention eliminates the above-mentioned problems and provides a reliable and effective metal extraction device. There is a purpose to what you do. Other objects and advantages of the invention will become apparent below.
上に述へた目的および他の目的に鑑み、本発明はひとつの特徴において以下の手 段を含む金属回収セルにある。In view of the above-mentioned and other objects, the present invention provides, in one aspect, the following steps. in a metal recovery cell containing stages.
細長い内周の回りに設けられた導電性表面を有する細長いハウジング、前記ハウ ジングに伸びる電極、 前記ハウジングに対する流体インレット、前記流体インレットから離れた前記ハ ウジングからの流体アウトレット、および、 前記電極および前記導電性表面に電気回路を接続するための電気端子。an elongated housing having a conductive surface about an elongated inner circumference; electrodes that extend into the ring, a fluid inlet relative to the housing; a fluid inlet remote from the fluid inlet; a fluid outlet from the using, and an electrical terminal for connecting an electrical circuit to the electrode and the electrically conductive surface;
好ましくは、細長いハウジングは端壁間に伸び、電極は前記ハウジング内に設け られて前記端壁間に伸びる。電極は電気陽極として利用され、導電性表面は陰極 として利用されることにより、ハウジング内で保持される液体の電解によって製 造される金属材料が導電性表面に堆積されることが好ましい。勿論、希望されれ ば電極が陰極として使用されても良く、そのときは金属材料はその上に堆積され る。希望されれば電極は流体中に渦巻きの流れを促進するために突起、あるいは リプのような表面処理を含むように形成されても良い。Preferably, the elongated housing extends between the end walls and the electrode is disposed within said housing. and extending between the end walls. The electrode is used as an electrical anode, and the conductive surface is used as a cathode. The product is produced by electrolysis of the liquid held within the housing. Preferably, the metallic material to be fabricated is deposited on the electrically conductive surface. Of course, it is hoped for. Alternatively, the electrode may be used as a cathode, on which the metallic material is deposited. Ru. If desired, the electrodes may have protrusions, or It may also be formed to include a surface treatment such as lipstick.
適切にはハウジングは導電性材料から形成される細長い円筒状の部分を含み、そ の導電性表面はそれと一体であっても良い。陰極および特に導電性材料は、堆積 する金属と同じになるように選択される。例えば、鋼の電解採集において、円筒 状の部分は薄い壁の銅の形をとり、その内部で銅の厚い層が堆積し、円筒状の部 分が新たな銅のチューブによって置換される。これによって、チューブから堆積 された金属を剥がす難しいプロセスを実施する必要性が無くなる。それに代えて 、導電性材料がその表面特性において導電性材料の上に作られる金属の層がそれ から従来の方法において分離される程度に電解採集される金属と相違するように 選択されても良い。適切には分離された金属が導電性材料から分離した後に同じ 材料の層を継続して堆積するために「出発」チューブとして利用される薄い壁の チューブの形であっても良い。例えば、銅の電解採集において他のセルのために 大量の銅の出発チューブがステンレス鋼のチューブを使用する比較的少数のセル から製造されても良い。Suitably the housing includes an elongated cylindrical portion formed from an electrically conductive material; The conductive surface of may be integral therewith. The cathode and especially the conductive material are deposited selected to be the same as the metal. For example, in electrolytic sampling of steel, cylindrical The shaped part takes the form of thin-walled copper, inside which a thick layer of copper is deposited, forming a cylindrical part. minutes is replaced by a new copper tube. This allows the deposit to be removed from the tube. Eliminates the need to carry out a difficult process of stripping the stained metal. instead of that , a layer of metal made on top of a conductive material is characterized by its surface properties. Unlike metals that are electrolytically harvested to the extent that they are separated in conventional methods from May be selected. Suitably the same after the separated metal is separated from the conductive material A thin-walled tube used as a "starting" tube to deposit successive layers of material. It may be in the form of a tube. For example, for other cells in copper electrowinning Large amounts of copper starting tubes, relatively few cells using stainless steel tubes It may be manufactured from.
流体インレットと流体アウトレットは、ハウジングの長さ方向の寸法に並列にな るようなハウジングに対するある方向に設けられる。しかし、流体インレットは ハウジングの第1の端部に隣接し、細長いハウジングの軸に実質的に垂直になり 、かつ/あるいはハウジングと電極との間に形成される環状の空洞に接するよう に配置され、それによって液体の環状の空洞を流れる螺旋状の流れが誘起される 。そのような螺旋状の流れは、電解採集された金属の堆積をも促進すると考えら れる。適切には流体アウトレットは流体インレットと類似した形状で、それから 離れて設けられ、液体の螺旋状の流れが更に高められる。The fluid inlet and fluid outlet are parallel to the longitudinal dimension of the housing. oriented in a direction relative to the housing such that However, the fluid inlet adjacent the first end of the housing and substantially perpendicular to the axis of the elongated housing; , and/or in contact with the annular cavity formed between the housing and the electrode. , which induces a spiral flow of liquid through the annular cavity. . Such a spiral flow is thought to also promote the deposition of electrolytically harvested metals. It will be done. Suitably the fluid outlet has a similar shape to the fluid inlet, and They are spaced apart to further enhance the helical flow of liquid.
流体インレットは第2の金属抽出セルの流体アウトレットに接続されても良く、 それによって流体は両方のセルを介して直列に通過し、流体からの金属の抽出を 高める。抽出バッテリーが直列に接続された複数のセルによって形成されても良 く、金属抽出が、ある持続時間にわたっである量の流体から生じ、それによって 希望する金属の全初期濃度の有意義な割合が抽出される。The fluid inlet may be connected to a fluid outlet of the second metal extraction cell; The fluid is thereby passed through both cells in series, leading to the extraction of metals from the fluid. enhance An extraction battery may be formed by multiple cells connected in series. In most cases, metal extraction occurs from a volume of fluid over a period of time, thereby A significant proportion of the total initial concentration of the desired metal is extracted.
抽出プロセスがガス状の副産物を発生する場合、ガス分離装置がセルの間に設け られ、上流のセルで発生したガスが密度差の技術、あるいは、それに類似した技 術によって下流のセルに入る前に液体から除去される。それに代えて、あるいは 、それに加えてセルの上方端部は換気用の開口を有しても良く、それによって発 生したガスは下流のセルに液体が入る前にセルから換気される。ガス分離効果は 液体アウトレットの上にガス分離室を設けることによって高められる。適切には 希望するレベルの有効性のために分離室は環状空洞の外径と略同じ直径であるべ きであり、その直径の1/2に等しい最小の高さを有する。If the extraction process produces gaseous by-products, a gas separator may be installed between the cells. The gas generated in the upstream cell is processed using density difference technology or similar technology. removed from the fluid before entering downstream cells. In lieu of that, or , in addition the upper end of the cell may have an opening for ventilation, thereby The produced gas is vented from the cell before liquid enters the downstream cell. The gas separation effect is Enhanced by providing a gas separation chamber above the liquid outlet. properly For the desired level of effectiveness, the separation chamber should have approximately the same diameter as the outside diameter of the annular cavity. and has a minimum height equal to 1/2 of its diameter.
セルは希望する限度内において、流体速度と陰極電流密度を含むセルの動作条件 を調整することによって、特殊な形で金属を電解採取するように適応させられ、 電解採取された少なくとも幾らかの金属は、陰極に堆積される代わりにセルを通 って液体流により運ばれ、ハウジングの円筒状の部分から離れた便宜的な収集点 において採取されても良い。セルは金属採集手段を有しても良く、それによって 少なくとも幾らかの電解採取された金属が電解採集プロセスに対する妨害を最小 にして粒子としてセルから抽出される。それに加えて、あるいは代わりに粒子収 集手段は、直列に接続されたセルの間に設けられても良く、ガス分離手段と一体 に形成されても良い。粒子収集手段は分離するために重量効果、あるいは遠心分 離効果を利用する分離手段を含んでも良く、かつ、収集室、あるいはホッパーを 含んでも良い。後者は外部弁手段によって外部収集領域に選択的に接続でき、ま た、収集室はセル、あるいは収集室から他の弁手段によって選択的に分離され、 それによって粒材料が開放した他の弁手段を介して閉じた外部弁手段を有する収 集室へ落下させ、それから他の弁手段を閉じるとともに外部弁手段を開くことに よって抽出される。Cell operating conditions, including fluid velocity and cathodic current density, within desired limits. adapted to electrowinning metals in a special form by adjusting the At least some of the electrowinning metal is passed through the cell instead of being deposited on the cathode. is carried by the liquid stream and has a convenient collection point separate from the cylindrical part of the housing. It may be collected at The cell may have metal harvesting means, thereby At least some electrowinning metals cause minimal interference to the electrowinning process. and then extracted from the cell as particles. Additionally or alternatively, particle collection The collecting means may be provided between cells connected in series and may be integrated with the gas separating means. may be formed. Particle collection means can be gravity effect or centrifugal to separate It may also include a separating means that utilizes a separation effect, and a collection chamber or hopper. May be included. The latter can be selectively connected to an external collection area by external valve means, or and the collection chamber is selectively separated from the collection chamber by a cell or other valve means; Thereby, the grain material is transferred to the container having the external valve means closed via the other valve means being opened. dropping into the collection chamber and then closing the other valve means and opening the external valve means. Therefore, it is extracted.
他の実施例において、収集手段はセル、あるいは分離室の下の収集位置とセルあ るいは分離室から離れた放出位置との間で移動可能な収集室を含む。適切には複 数の収集室か設けられ、回転マガジンの周りに配置され、後者が回転して収集室 か収集位置と放出位置の間で移動させられる。In other embodiments, the collection means includes a cell or a collection location below the separation chamber and the cell or or a collection chamber movable between the separation chamber and a remote discharge location. Appropriately multiple Several collection chambers are provided, arranged around a rotating magazine, the latter rotating to open the collection chambers. or moved between collection and release positions.
他の観点において、本発明は以下の工程を含む金属を電解採取する方法にある。In another aspect, the invention is a method of electrowinning a metal, comprising the steps of:
内周に配置された導電性表面を有する細長いハウジングと、前記ハウジング内に 設けられた細長い電極と、前記ハウジングに対する流体インレットと前記流体イ ンレットから離れた前記ハウジングからの流体アウトレット、前記電極および前 記導電性回路に電気回路を接続するための一対の電気終端を含む金属抽出装置を 設ける工程、 前記導電性表面および前記電極の間に電流源を接続する工程、および、前記流体 インレットおよび前記流体アウトレットの間の前記ハウジングを介して金属の分 解塩を含む流体を通す工程。an elongated housing having a conductive surface disposed about an inner periphery; an elongate electrode provided, a fluid inlet for the housing and a fluid inlet for the housing; a fluid outlet from the housing remote from the outlet, the electrode and the A metal extraction device containing a pair of electrical terminations for connecting an electrical circuit to a conductive circuit. the process of providing; connecting a current source between the conductive surface and the electrode; and metal dispensing through the housing between the inlet and the fluid outlet; The process of passing a fluid containing salt removal.
この方法は、電解採取プロセスに波山プロセスを加えても良く、その流体は電解 採取される金属を含む鉱石微粒子を含むことにより、金属粒子を分解するプロセ スが波山と電解採取の別々のステップを必要とする代わりに電解採取プロセスと 同時に実施される。例えば、鉱石から銅を電解採取するときに細かく粉砕された 鉱石がセル、あるいは複数のセルを通る硫酸の稀釈溶液に入れられる。銅は酸中 て分解し、溶液から電解採取され、チューブ壁状に堆積し、その間硫酸は再生さ れる。鉱石の残りは分解されず、かつ、沈澱、濾過、あるいは遠心効果によって 液体から分離される。In this method, a wave mountain process may be added to the electrowinning process, and the fluid is electrolyzed. The process of decomposing metal particles by including ore fine particles containing the metals being extracted. electrowinning process instead of requiring separate steps of wave peak and electrowinning. will be carried out simultaneously. For example, when copper is electrowinning from ore, it is finely ground. The ore is placed in a dilute solution of sulfuric acid that passes through the cell or cells. copper in acid The sulfuric acid is decomposed, electrowinning from the solution, and deposited on the tube wall, during which time the sulfuric acid is regenerated. It will be done. The remainder of the ore remains undecomposed and is removed by sedimentation, filtration, or centrifugal effects. separated from the liquid.
本発明がもっと簡単に理解され、実用的にされるために本発明の実施例を示す添 付した図面が参照される。In order that the present invention may be more easily understood and put into practical use, the following appendix presents examples of the present invention. Reference is made to the attached drawings.
図1は、本発明による電解採取セルの断面側面図である。FIG. 1 is a cross-sectional side view of an electrowinning cell according to the invention.
図2は、図1に示された電解採取セルの断面平面図である。FIG. 2 is a cross-sectional plan view of the electrowinning cell shown in FIG. 1. FIG.
図3は、本発明の他の実施例の断面側面図である。FIG. 3 is a cross-sectional side view of another embodiment of the invention.
図4は、本発明による分離装置の断面側面図である。FIG. 4 is a cross-sectional side view of a separation device according to the invention.
図1および2に示された電解セルlOは、金属チューブ12を含むハウジング組 立体11を含み、その外周に対して上方端部キャップ13および下方端部キャッ プ14がシーリングリング15によってシールされている。ハウジング組立体1 1は、端部キャップ13および14において形成されたフランジ17にクランプ された貫通ボルト16によって一緒に保持されている。The electrolytic cell lO shown in FIGS. 1 and 2 includes a housing assembly including a metal tube 12. The solid body 11 has an upper end cap 13 and a lower end cap around its outer circumference. The pipe 14 is sealed by a sealing ring 15. Housing assembly 1 1 is clamped to flanges 17 formed in the end caps 13 and 14. are held together by a through bolt 16.
シーリンググランド20は端部キャップ13および14において中心に形成され 、円筒状電極21がそれを通っている。希望されればひとつだけのシーリンググ ランドが設けられても良く、電極21が端部キャップから内方へ突出するチュー ブ状のリセス内に、あるいは、ボスの周りに他の端部において終端させられても 良く、チューブ状電極21はボスあるいはリセスにシーリング手段によってシー ルされるか、あるいは電極21を通る流体の損失を最小にするようにブロックさ れる。液体アウトレット22が上方端部キャップ13に形成さ札液体インレット 23が下方端部キャップ14に形成されている。アウトレット22とインレット 23はハウジング組立体11の軸に垂直で、ハウジング組立体11と電極21の 間に形成された環状空洞24に接した軸と一線になっている。下方端部キャップ 14にインレット23を位置させることによって誘導される液体の上方の流れは 上方端部キャップ13に形成されたガス換器32に向かって電極21の上に堆積 するガスを取り除く傾向があり、そのガス流は液体の流れを高めて外部のポンプ の要件を減らすために泡のポンプとして動作する。勿論、希望されればインレッ ト23は上方端部キャップ13に形成されても良く、アウトレット22は下方の 液体の流れを誘導するために下方端部キャップ14に形成されても良い。A sealing gland 20 is centrally formed in the end caps 13 and 14. , a cylindrical electrode 21 passes through it. Only one sealing ring available if desired Lands may be provided, and the electrodes 21 extend inwardly from the end caps of the tubes. terminated at the other end in a tubular recess or around a boss. Preferably, the tubular electrode 21 is sealed to the boss or recess by sealing means. or blocked to minimize loss of fluid through electrode 21. It will be done. A liquid outlet 22 is formed in the upper end cap 13. 23 is formed on the lower end cap 14. Outlet 22 and inlet 23 is perpendicular to the axis of the housing assembly 11 and connects the housing assembly 11 and the electrode 21. It is in line with the axis tangential to the annular cavity 24 formed therebetween. lower end cap The upward flow of liquid induced by positioning the inlet 23 at 14 is Deposited on the electrode 21 towards the gas exchanger 32 formed in the upper end cap 13 The gas flow increases the liquid flow and is used by external pumps. Acts as a foam pump to reduce requirements. Of course, if you wish, you can An outlet 23 may be formed in the upper end cap 13 and an outlet 22 in the lower end cap 13. A lower end cap 14 may be formed to direct liquid flow.
インレット22とチューブ12の下方端部の間の領域において、下方端部キャッ プ14の内径はチューブ12の内径に密接して整合するように形成され、その結 果、比較的平滑な円筒状表面が入って来る液体の螺旋の流れを高めるために設け られる。同じプロセスの直径の整合が上方端部キャップ13と環状空洞24の平 滑な螺旋状の流れを更に高めるために、チューブ12に適用される。In the area between the inlet 22 and the lower end of the tube 12, the lower end cap The inner diameter of tube 14 is formed to closely match the inner diameter of tube 12, and its As a result, a relatively smooth cylindrical surface is provided to enhance the helical flow of the incoming liquid. It will be done. The same process of matching the diameters of the upper end cap 13 and the annular cavity 24 applied to the tube 12 to further enhance the smooth spiral flow.
端部キャップ13と14のそれぞれは、フランジアダプター25、ある長さのパ イプ26、パイプキャップ27、圧縮フィッティング30およびある長さの小さ な直径のバイブ31を含むポリ塩化ビニール(PVC) 、プラスチックバイブ フィッティングの組立体から形成され、これらの要素は一体に溶接されるか、あ るいはにかオ)でくっつけられる。勿論、希望されれば端部キャップはプラスチ ックモールドプロセスによって一体に形成されても良い。希望されればガス換器 32はガスが上方端部キャップ13に収集されたときに開き、ガスか換気された 後に閉じるフロート弁、あるいはそれらの同等のものを有しても良い。Each of the end caps 13 and 14 has a flange adapter 25, a length of the pipe 26, pipe cap 27, compression fitting 30 and a length of small Polyvinyl chloride (PVC), plastic vibrator, including vibrator 31 with a diameter of Formed from an assembly of fittings, these elements may be welded together or Ruihanikao) can be attached. Of course, the end caps can be made of plastic if desired. It may also be integrally formed by a pack molding process. Gas exchanger if desired 32 opens when gas is collected in the upper end cap 13 and the gas is vented. It may also have a float valve that closes later, or the equivalent thereof.
硫酸と硫化銅を含む液体から電解銅を採取することが要求されれば、銅チューブ が金属チューブ+2として利用され、チューブ状の電極21が表面被覆の貴金属 酸化物を有するチタニウム(寸法的に安定な陽極として知られる)、あるいは鉛 アンチモン合金のような動作条件下において酸に溶けず、かつ、特性が変化しな い他の材料から形成されても良い。その代わりに金属チューブ12は、沈着材料 が容易に除去されるステンレス鋼のような不活性材料から形成されても良い。Copper tubing if required to extract electrolytic copper from liquids containing sulfuric acid and copper sulfide is used as the metal tube +2, and the tube-shaped electrode 21 is made of noble metal with a surface coating. Titanium with oxide (known as a dimensionally stable anode) or lead It is insoluble in acids and its properties do not change under operating conditions like antimony alloys. It may also be formed from other materials. Instead, the metal tube 12 is made of deposited material. It may be formed from an inert material such as stainless steel, which is easily removed.
使用において、直流電力源チューブ状電極21に接合される正の端子を存するセ ルIOに接続され、それは陽極となり、金属チューブ12に接合される負の端子 を有するセルlOに接続され、それは陰極となり、ハウジング12の組立および 分解および特に取外しと取替えを容易にするため、クリップオンコネクターが使 用されることが好ましい。電極21とチューブ12の間を通る電流はチューブ1 2の上に銅を堆積し、そのプロセスによって溶液から放出される酸素はガス換器 32を経て大気へ換気される。銅の希望した厚さがチューブ12の内側に形成さ れると、精錬された銅として販売のために、あるいは電気ブスバーとして使用の ために除去され、新しいチューブと取り替えられる。In use, the DC power source has a positive terminal connected to the tubular electrode 21. the negative terminal is connected to the metal tube 12, which becomes the anode, and the negative terminal is joined to the metal tube 12. is connected to a cell lO having a Clip-on connectors are used to facilitate disassembly and especially removal and replacement. It is preferable to use The current passing between the electrode 21 and the tube 12 2, the oxygen released from the solution by the process is removed by a gas exchanger. 32 to the atmosphere. The desired thickness of copper is formed inside the tube 12. Once refined, copper can be sold as refined copper or used as electric busbars. removed and replaced with a new tube.
希望されればアレイ状のセル10が作られても良く、かつ、液体が直列の複数の セルを通してポンプされ、液体の鋼の量が前進的に減少させられる。勿論、アレ イ状のセルの間の直列かつ並列の希望する形状の流れが形成され、それによって セルにおける流れの状態か最適にさせられる。同じようにセルに対する電源か所 望の直列、並列あるいは直並列の形で構成され、それによってセル電流と電圧を 利用可能な電源に整合させる。If desired, an array of cells 10 may be created, and the liquid may be connected to a plurality of cells in series. Pumped through the cell, the amount of liquid steel is progressively reduced. Of course, that A series and parallel flow of the desired shape between the A-shaped cells is formed, thereby Flow conditions in the cell are optimized. Similarly, the power source for the cell can be configured in the desired series, parallel or series-parallel configuration, thereby controlling the cell current and voltage. Match available power.
図3に示される電解セル40は、形状において図1および図2に示されるものに 類似しているが、上方端部キャップ41においてチューブ42の内径の半分より 大なる垂直ギャップか液体アラ1−レット43とガス換器44の間に残され、チ ューブ42を介して立ちトがる流体に含まれるガスは、後者がセル40から取り 出される前に液体から分離されても良い。下方端部キトツブ45もまた、液体イ ンレット46の底部と下方端部キャップ45のベース47の間でデユープ42の 内径の半分より大きな垂直ギャップを有するように形成される。陽極50は液体 イン1ノッ1−46の上で終端するが、円筒状の形状はベース47に取り付けら れた導電性でない陽極マウント51によって液体インレット46を超えて下方ま で続いており、インレットの流れのパターンは目立つ程には妨害されない。これ らの特徴は、セル40の底部に落ちる金属粒子の穏やかな形成によりインI/ ツ)−46を介した液体の流れを阻害しないか、あるいは陽極50とチューブ4 2の間の電気的ショートを作らないようにすることを保証する。The electrolytic cell 40 shown in FIG. 3 is similar in shape to that shown in FIGS. 1 and 2. Similar, but less than half the inner diameter of the tube 42 at the upper end cap 41 A large vertical gap may be left between the liquid airflow 1-let 43 and the gas exchanger 44; The gas contained in the fluid rising through the tube 42 is removed by the latter from the cell 40. It may be separated from the liquid before being served. The lower end knob 45 also contains liquid The duplex 42 is located between the bottom of the outlet 46 and the base 47 of the lower end cap 45. Formed with a vertical gap greater than half the inner diameter. Anode 50 is liquid The cylindrical shape is attached to the base 47 and terminates above the in-1 knot 1-46. The non-conductive anode mount 51 extends downwardly beyond the liquid inlet 46. continues, and the inlet flow pattern is not appreciably disturbed. this These characteristics are due to the gentle formation of metal particles that fall to the bottom of the cell 40. t) Do not obstruct the flow of liquid through the anode 50 and the tube 4. This ensures that no electrical shorts are created between the two.
下方端部ギャップ45とチューブ42の下方端部の間の円周状の接合は、少なく ともインレット46の頂部を超えてチューブ42の内径の半分にわt:って設け られ、インレットの近くの撹乱された流れの状態におけるチューブ42の端部の 腐蝕か最小にさせられる。上方端部キャップ41とチューブ42の上方端の間の 円周状の接合は、同じように形状を与えられ、螺旋状の出口の流れの平滑さが高 められ、かつ、チューブ42の上方端の腐蝕が最小にさせられる。The circumferential junction between the lower end gap 45 and the lower end of the tube 42 is at least It is provided beyond the top of the inlet 46 and half the inner diameter of the tube 42. of the end of tube 42 in turbulent flow conditions near the inlet. Corrosion is minimized. between the upper end cap 41 and the upper end of the tube 42. Circumferential junctions are similarly shaped and have a high smoothness of the helical exit flow. and corrosion of the upper end of tube 42 is minimized.
図4に示された分離装置160は、セルlOに形成された金属粒子を除去するた めに利用されるが、陰極の上には堆積されず、この目的のために垂直バッフル6 2によってふたつの部分に分けられ、頂部において閉じられた垂直のチューブ状 の分離室61を含み、後者はアウトレットバイブロ4からインレットバイブロ3 を分離する。希望されればフロート弁を含んでも良いガス換器65は、分離室6 1の上方部に形成されている。その下方端において分離室61は円錐状に内側に 向かってテーパーを有しており、上方弁66において終端し、その下方面がチュ ーブ状収集室67に取り付けられている。後者は下方弁70によってその下方端 部において終端させられている。The separation device 160 shown in FIG. 4 is used to remove metal particles formed in the cell IO. vertical baffle 6 for this purpose. A vertical tube divided into two parts by 2 and closed at the top. The latter includes a separation chamber 61 from the outlet vibro 4 to the inlet vibro 3. Separate. A gas exchanger 65, which may include a float valve if desired, is connected to the separation chamber 6. It is formed in the upper part of 1. At its lower end, the separation chamber 61 is conically shaped inwards. It tapers toward the upper valve 66 and terminates at the upper valve 66, the lower surface of which is the tube. It is attached to a tube-shaped collection chamber 67. The latter is connected to its lower end by a lower valve 70. It is terminated at the end.
使用において、ガスの泡と金属の粒子を運ぶ液体は、インレットバイブロ3を介 してセルlOの液体アウトレット22から分離装置60へ入っても良い。分離室 61の容量はセルlOの容量の多数倍にさせられ、液体は比較的長い対流時間F IGURE 2 FIGURE 3 FIGURE 4 補正書の翻訳文提出書(特許法第184条の8)平成5年8月13日lIn use, the liquid carrying gas bubbles and metal particles is passed through the inlet vibro 3. The liquid may then enter the separation device 60 through the liquid outlet 22 of the cell IO. separation room The volume of 61 is made to be many times the volume of cell lO, and the liquid has a relatively long convection time F IGURE 2 FIGURE 3 FIGURE 4 Submission of translation of written amendment (Article 184-8 of the Patent Law) August 13, 1993 l
Claims (20)
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CL2018003073A1 (en) * | 2018-10-29 | 2018-11-30 | Gallegos Riedemann Alejo | Process of redox reduction of dissolved metals by controlling the cathodic potential and / or dimensionless ratio, varying flows and currents |
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DE717484C (en) * | 1938-01-15 | 1942-02-16 | Siemens Ag | Device for electrolyte drainage during the electrolytic deposition of metals |
DE1136122B (en) * | 1957-09-26 | 1962-09-06 | Coussinets Ste Indle | Process and device for the electrolytic production of copper-lead powder |
GB916438A (en) * | 1960-08-15 | 1963-01-23 | Kodak Ltd | A high current density silver recovery unit |
FR1374037A (en) * | 1962-11-15 | 1964-10-02 | Ciba Geigy | Advanced cell for the electrolysis of molten products |
FR2299667A1 (en) * | 1975-01-29 | 1976-08-27 | Lakehal Denis | Electrolytic cell for recovery of silver from photographic chemicals - using intense agitation and high current density |
US4026784A (en) * | 1975-11-10 | 1977-05-31 | Rivers James R | Metal recovery unit |
JPS55145189A (en) * | 1979-04-30 | 1980-11-12 | Kimura Etsuchingu Kenkyusho:Kk | Electrolytic treating apparatus of waste liquid containing silver |
US4439300A (en) * | 1983-04-01 | 1984-03-27 | General Dental, Inc. | Vortex type metal collector |
NO164921C (en) * | 1987-05-27 | 1990-11-28 | Cheminvest As | PROCEDURE FOR ELECTRICAL EXTRACTION OF METAL AND DEVICE FOR CARRYING OUT THE PROCEDURE. |
US5017273A (en) * | 1989-03-23 | 1991-05-21 | Gunter Woog | Disposable cell for recovering conductive metal and method of using |
AU620868B2 (en) * | 1988-05-20 | 1992-02-27 | Gunter Woog | Disposable cell for recovering conductive metal and method of use |
US4840717A (en) * | 1988-08-24 | 1989-06-20 | Dzodin Milton A | Silver recovery cell |
-
1992
- 1992-02-12 DK DK92904768T patent/DK0571467T3/en active
- 1992-02-12 US US08/104,144 patent/US5529672A/en not_active Expired - Lifetime
- 1992-02-12 CZ CS931670A patent/CZ167093A3/en unknown
- 1992-02-12 BR BR9205643A patent/BR9205643A/en not_active IP Right Cessation
- 1992-02-12 JP JP50478392A patent/JP3327922B2/en not_active Expired - Lifetime
- 1992-02-12 RU RU93054000A patent/RU2114935C1/en active
- 1992-02-12 SK SK880-93A patent/SK88093A3/en unknown
- 1992-02-12 HU HU9302349A patent/HUT65003A/en unknown
- 1992-02-12 CA CA002104120A patent/CA2104120C/en not_active Expired - Lifetime
- 1992-02-12 AU AU12581/92A patent/AU651439B2/en not_active Expired
- 1992-02-12 ES ES92904768T patent/ES2112313T3/en not_active Expired - Lifetime
- 1992-02-12 WO PCT/AU1992/000052 patent/WO1992014865A1/en not_active Application Discontinuation
- 1992-02-12 AT AT92904768T patent/ATE159990T1/en not_active IP Right Cessation
- 1992-02-12 RO RO93-01790A patent/RO112899B1/en unknown
- 1992-02-12 DE DE69223040T patent/DE69223040T2/en not_active Expired - Lifetime
- 1992-02-12 EP EP92904768A patent/EP0571467B1/en not_active Expired - Lifetime
-
1993
- 1993-08-13 FI FI933579A patent/FI933579A/en not_active Application Discontinuation
- 1993-08-13 NO NO932896A patent/NO305965B1/en not_active IP Right Cessation
- 1993-08-13 OA OA60400A patent/OA09864A/en unknown
- 1993-09-09 BG BG98102A patent/BG61950B1/en unknown
-
1998
- 1998-02-04 GR GR980400215T patent/GR3026047T3/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003505598A (en) * | 1999-07-21 | 2003-02-12 | エレクトロメタルズ テクノロジーズ リミテッド | Method and apparatus for electrolytic extraction of powdered metal from solution |
Also Published As
Publication number | Publication date |
---|---|
AU1258192A (en) | 1992-09-15 |
RO112899B1 (en) | 1998-01-30 |
GR3026047T3 (en) | 1998-05-29 |
DE69223040T2 (en) | 1998-06-10 |
JP3327922B2 (en) | 2002-09-24 |
OA09864A (en) | 1994-08-15 |
HU9302349D0 (en) | 1993-10-28 |
US5529672A (en) | 1996-06-25 |
WO1992014865A1 (en) | 1992-09-03 |
SK88093A3 (en) | 1994-01-12 |
BR9205643A (en) | 1994-06-21 |
CA2104120A1 (en) | 1992-08-15 |
ES2112313T3 (en) | 1998-04-01 |
BG98102A (en) | 1995-01-31 |
BG61950B1 (en) | 1998-10-30 |
DK0571467T3 (en) | 1998-07-27 |
NO932896L (en) | 1993-10-13 |
HUT65003A (en) | 1994-03-28 |
EP0571467B1 (en) | 1997-11-05 |
ATE159990T1 (en) | 1997-11-15 |
EP0571467A4 (en) | 1993-12-15 |
NO932896D0 (en) | 1993-08-13 |
EP0571467A1 (en) | 1993-12-01 |
RU2114935C1 (en) | 1998-07-10 |
FI933579A0 (en) | 1993-08-13 |
AU651439B2 (en) | 1994-07-21 |
FI933579A (en) | 1993-10-05 |
CZ167093A3 (en) | 1994-02-16 |
DE69223040D1 (en) | 1997-12-11 |
NO305965B1 (en) | 1999-08-23 |
CA2104120C (en) | 2004-01-20 |
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